Associate Director, Global Clinical Supply Chain

Overview

Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value.

The Company strives to discover and develop first-in-class and best-in-class medicines-advancing a diverse portfolio of large and small molecules.

Job Summary (Primary function)

The Associate Clinical Supply Director manages clinical supply chain of compounds in the clinical stage of development, and focuses on process change within Investigational Material Supply Chain (IMSC) in close collaboration with internal and external subject matter experts (SMEs).

Essential Functions of the Job (Key responsibilities)

• As a key interface and SME for IMSC Operations, drive process change and improvement initiatives with contracted CMOs, Technical Operations, Medical Affairs, Quality and Clinical Operations, etc., as needed, to ensure effectiveness and efficiency.
• Support training, development and mentoring indirect reports, as needed.
• Develop strong internal collaboration with stakeholders, such as Clinical Operations, Project Management, Regulatory, Medical Affairs, Quality and Technical Operation functions to ensure successful delivery of clinical supply.
• Act as a key interface between the Contract Manufacturing Organization (CMO) and clinical teams, serving as a point of escalation, for clinical supply issues, ensuring clear communication and collaboration across diverse teams.
• Manage all aspects of clinical study requirements and Clinical Packaging activities.
• In collaboration with Clinical / Technical Operations and Project management, establish and meet timelines for clinical supplies available for clinical trials, managing inventory of clinical supplies before and during clinical studies.
• Identify external packaging sites, monitors external clinical packaging, and reviews master batch records.
• Coordinate GMP auditing activities at CMOs.
• Provide management with accurate time frames for resolution of delays in obtaining supplies for clinical projects.
• Recommend insight and recommendations into procedural improvements, as needed, and assist in the implementation of the improvements.
• Develop and manage strategic alliances with contract partners for procurement, packaging, transportation, brokerage, storage and distribution.

Qualifications (Minimal acceptable level of education, work experience, and competency)

Disclaimer : The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.

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